About The Position
CSL Behring is a global biotherapeutics leader driven by our promise to save lives. Focused on serving patients’ needs by using the latest technologies, we discover, develop and deliver innovative therapies for people living with conditions in the immunology, hematology, cardiovascular and metabolic, respiratory, and transplant therapeutic areas. We use three strategic scientific platforms of plasma fractionation, recombinant protein technology, and cell and gene therapy to support continued innovation and continually refine ways in which products can address unmet medical needs and help patients lead full lives. CSL Behring operates one of the world’s largest plasma collection networks, CSL Plasma. Our parent company, CSL, headquartered in Melbourne, Australia, employs 32,000 people, and delivers its lifesaving therapies to people in more than 100 countries. To learn more about CSL, CSL Behring, CSL Seqirus and CSL Vifor visit https://www.csl.com/ and CSL Plasma at https://www.cslplasma.com/. For more information on CSL benefits visit How CSL Supports Your Well-being | CSL. You Belong at CSL At CSL, Inclusion and Belonging is at the core of our mission and who we are. It fuels our innovation day in and day out. By celebrating our differences and creating a culture of curiosity and empathy, we are able to better understand and connect with our patients and donors, foster strong relationships with our stakeholders, and sustain a diverse workforce that will move our company and industry into the future. To learn more about inclusion and belonging visit https://www.csl.com/careers/inclusion-and-belonging Equal Opportunity Employer CSL is an Equal Opportunity Employer. If you are an individual with a disability and need a reasonable accommodation for any part of the application process, please visit https://www.csl.com/accessibility-statement.
Requirements
- Bachelors Degree in Life Sciences, Engineering, Logistics or equivalent experience
- 5+ years of experience in clinical supply management with the pharmaceutical industry
- Demonstrated knowledge of ICH-GCP regulations and the conduct of clinical studies
- Demonstrated knowledge of cGMP and cGDP regulations
- Team-player with proven effective interpersonal and communication skills
Responsibilities
- Ensure efficient, cost-effective clinical trial supply planning and management for low to medium complexity studies
- Performs planning and forecasting of drug volume requirements
- Sample collection and analysis
- Ensures proper storage, transportation and archiving
- Assists with selection and management of external service providers in compliance with outsourcing strategy to ensure cost efficient and high quality services
- Leverages interactive response technology (IRT) system to support clinical supply management activities
- Authors/reviews critical study documents (e.g. study protocol, product dossiers, handling instructions, study reports)
- Leads or participates in global Clinical Trial Supply project meetings with internal and external team members
- Partners with R&D and other functions to ensure optimal use of systems and processes to support clinical trial supply chain
- Supports continuous improvements in clinical drug supply and revises SOPs to ensure ongoing compliance and efficient conduct of clinical trial supply activities
Benefits
- Relocation and mobility assistance are not provided
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
